|
ENST00000356955.7:c.751C>T
(ADAM15)
MANE Select
|
ENSP00000349436.2:p.Arg251Trp
|
|
|
ENST00000271836.10:c.751C>T
(ADAM15)
|
ENSP00000271836.6:p.Arg251Trp
|
|
|
ENST00000355956.6:c.751C>T
(ADAM15)
|
ENSP00000348227.2:p.Arg251Trp
|
|
|
ENST00000356955.6:c.751C>T
(ADAM15)
|
ENSP00000349436.2:p.Arg251Trp
|
|
|
ENST00000359280.8:c.751C>T
(ADAM15)
|
ENSP00000352226.4:p.Arg251Trp
|
|
|
ENST00000360674.8:c.751C>T
(ADAM15)
|
ENSP00000353892.4:p.Arg251Trp
|
|
|
ENST00000368412.7:c.751C>T
(ADAM15)
|
ENSP00000357397.3:p.Arg251Trp
|
|
|
ENST00000368413.5:c.278-1113C>T
(ADAM15)
|
ENSP00000357398.1:n.278-1113C>T
|
|
|
ENST00000447332.3:c.703C>T
(ADAM15)
|
ENSP00000476000.1:p.Arg235Trp
|
|
|
ENST00000449910.6:c.751C>T
(ADAM15)
|
ENSP00000403843.2:p.Arg251Trp
|
|
|
ENST00000461564.6:n.881C>T
(ADAM15)
|
|
|
|
ENST00000470779.1:n.206C>T
(ADAM15)
|
|
|
|
ENST00000472434.5:n.787C>T
(ADAM15)
|
|
|
|
ENST00000473905.6:n.1029C>T
(ADAM15)
|
|
|
|
ENST00000480331.5:n.956C>T
(ADAM15)
|
|
|
|
ENST00000487956.6:n.749C>T
(ADAM15)
|
|
|
|
ENST00000526491.5:c.751C>T
(ADAM15)
|
ENSP00000432347.1:p.Arg251Trp
|
|
|
ENST00000527418.5:n.2397C>T
(ADAM15)
|
|
|
|
ENST00000529473.5:c.751C>T
(ADAM15)
|
ENSP00000434227.1:p.Arg251Trp
|
|
|
ENST00000531455.5:c.781C>T
(ADAM15)
|
ENSP00000432927.1:p.Arg261Trp
|
|
|
ENST00000534019.1:n.520C>T
(ADAM15)
|
|
|
|
NM_001261464.1:c.781C>T
(ADAM15)
|
NP_001248393.1:p.Arg261Trp
|
|
|
NM_001261465.1:c.751C>T
(ADAM15)
|
NP_001248394.1:p.Arg251Trp
|
|
|
NM_001261466.1:c.703C>T
(ADAM15)
|
NP_001248395.1:p.Arg235Trp
|
|
|
NM_003815.4:c.751C>T
(ADAM15)
|
NP_003806.3:p.Arg251Trp
|
|
|
NM_207191.2:c.751C>T
(ADAM15)
|
NP_997074.1:p.Arg251Trp
|
|
|
NM_207194.2:c.751C>T
(ADAM15)
|
NP_997077.1:p.Arg251Trp
|
|
|
NM_207195.2:c.751C>T
(ADAM15)
|
NP_997078.1:p.Arg251Trp
|
|
|
NM_207196.2:c.751C>T
(ADAM15)
|
NP_997079.1:p.Arg251Trp
|
|
|
NM_207197.2:c.751C>T
(ADAM15)
|
NP_997080.1:p.Arg251Trp
|
|
|
NR_040773.1:n.236-6725G>A
(DCST1-AS1)
|
|
|
|
NR_048577.1:n.866C>T
(ADAM15)
|
|
|
|
NR_048578.1:n.866C>T
(ADAM15)
|
|
|
|
NR_048579.1:n.866C>T
(ADAM15)
|
|
|
|
NM_001261464.2:c.781C>T
(ADAM15)
|
NP_001248393.1:p.Arg261Trp
|
|
|
NM_001261465.2:c.751C>T
(ADAM15)
|
NP_001248394.1:p.Arg251Trp
|
|
|
NM_001261466.2:c.703C>T
(ADAM15)
|
NP_001248395.1:p.Arg235Trp
|
|
|
NM_003815.5:c.751C>T
(ADAM15)
|
NP_003806.3:p.Arg251Trp
|
|
|
NM_207191.3:c.751C>T
(ADAM15)
|
NP_997074.1:p.Arg251Trp
|
|
|
NM_207194.3:c.751C>T
(ADAM15)
|
NP_997077.1:p.Arg251Trp
|
|
|
NM_207195.3:c.751C>T
(ADAM15)
|
NP_997078.1:p.Arg251Trp
|
|
|
NM_207196.3:c.751C>T
(ADAM15)
|
NP_997079.1:p.Arg251Trp
|
|
|
NM_207197.3:c.751C>T
(ADAM15)
MANE Select
|
NP_997080.1:p.Arg251Trp
|
|
|
NR_048577.2:n.822C>T
(ADAM15)
|
|
|
|
NR_048578.2:n.822C>T
(ADAM15)
|
|
|
|
NR_048579.2:n.822C>T
(ADAM15)
|
|
|
